Hippocampal-Avoiding Whole Brain Irradiation With Simultaneous Integrated Boost for Treatment of Brain Metastases
Phase II Trial of Hippocampal-Avoiding Whole Brain Irradiation With Simultaneous Integrated Boost for Treatment of Brain Metastases
Обзор исследования
Статус
Вмешательство/лечение
Подробное описание
Тип исследования
Регистрация (Действительный)
Фаза
- Фаза 2
Контакты и местонахождение
Места учебы
-
-
Texas
-
Dallas, Texas, Соединенные Штаты, 75390
- University of Texas Southwestern Medical Center
-
-
Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
Принимает здоровых добровольцев
Полы, имеющие право на обучение
Описание
Inclusion Criteria:
- Pathologically (histologically or cytologically) proven diagnosis of a non-hematopoietic malignancy other than small cell lung cancer and germ cell malignancy.. Direct biopsy of CNS (central nervous system) lesions is not necessarily required although could constitute an allowed site of tissue confirmation as medically prudent. Patients who have been disease free for more than 5 years prior to the appearance of CNS metastases should undergo repeat biopsy of either a systemic metastasis or the CNS metastases to confirm the recurrent malignancy.
- Patients with measurable brain metastasis outside a 5-mm margin around either hippocampus
- Patients with measurable brain metastasis who have not been or will not be treated with SRS (stereotactic radiosurgery ) or surgical resection (Note: These treatment options are only permitted at relapse)
- History/physical examination within 28 days prior to registration
- Patients must fall into RTOG (Radiation Therapy Oncology Group) recursive partitioning analysis (RPA) class I or II
- Patients must have a life expectancy of at least 4 months.
- Age ≥ 18 years
- Karnofsky performance status ≥ 70
- Patients must provide study-specific informed consent prior to study entry
- Women of childbearing potential and male participants must practice adequate contraception
- Women of childbearing potential must have a negative, qualitative serum pregnancy test ≤2 weeks prior to study entry
Exclusion Criteria:
- Patients with greater than 9 discrete metastases on MRI.
- Patients with leptomeningeal metastases
- Patients with measurable brain metastasis not resulting from small cell lung cancer and germ cell malignancy
- Plan for chemotherapy or targeted therapies during WBRT or over the subsequent 7 days
- Contraindication to MR (Magnetic resonance) imaging such as implanted metal devices or foreign bodies, severe claustrophobia AND patients unable to receive gadolinium contrast agents
- Serum creatinine > 1.4 mg/dl ≤ 28 days prior to study entry
- Prior radiation therapy to the brain
- Patients planning to undergo radiosurgery to any CNS lesion OR patients planning to have surgical resection of ALL of their CNS lesions
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Н/Д
- Интервенционная модель: Одногрупповое задание
- Маскировка: Нет (открытая этикетка)
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
|
Экспериментальный: Radiation
Whole-Brain Radiotherapy
|
Hippocampal-Avoiding Whole Brain Irradiation with Simultaneous Integrated Boost
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Mean Change in *Delayed* Recall Score by Hopkins Verbal Learning Test-Revised (HVLT-R DR) Score
Временное ограничение: Baseline, 3 months
|
The HVLT-R is a validated test to assess neurocognitive function and it incorporates 6 different forms, each including 12 nouns (targets) with 4 words drawn from 3 semantic categories. *Delayed*recall was measured by recalling the 12 targets after a 20-minute delay. 1 point is awarded for each successfully recalled target. There is no range- recalling more is more memory. Mean change was calculated by the following formula: 100*(3 month - baseline) / baseline |
Baseline, 3 months
|
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Mean Change in *Immediate* Recall Score by Hopkins Verbal Learning Test-Revised (HVLT-R)
Временное ограничение: Baseline, at 3 months
|
The HVLT-R is a validated test to assess neurocognitive function and it incorporates 6 different forms, each including 12 nouns (targets) with 4 words drawn from 3 semantic categories. *Immediate* recall was measured by memorizing a list of 12 targets for 3 consecutive trials. 1 point is awarded for each successfully recalled target. There is no range- recalling more is more memory. Mean change was calculated by the following formula: 100*(3 month - baseline) / baseline |
Baseline, at 3 months
|
|
Mean Change in *Delayed Recognition* Score by Hopkins Verbal Learning Test-Revised (HVLT-R)
Временное ограничение: Baseline, 3 months
|
The HVLT-R is a validated test to assess neurocognitive function and it incorporates 6 different forms, each including 12 nouns (targets) with 4 words drawn from 3 semantic categories. *Delayed recognition* was measured by using recognition discrimination index. 1 point is awarded for each successfully recalled target. There is no range- recalling more is more memory. Mean change was calculated by the following formula: 100*(3 month - baseline) / baseline |
Baseline, 3 months
|
|
Mean Change in Neurocognitive Function as Measured by Controlled Word Association Test
Временное ограничение: Baseline, at 3 months
|
Controlled Word Association Test (COWAT) is used to assess language and executive/frontal skills. The patient produces as many words as possible in 1 min. (each) for a specific letter (C, F, L or P, R, W). Requires about 5 min to complete. 1 point is awarded for each word produced. Mean change was calculated by the following formula: 100*(3 month - baseline) / baseline |
Baseline, at 3 months
|
|
Mean Change in Trail Making Test (TMT- A) Score
Временное ограничение: Baseline, at 3 months
|
Trail Making Test (TMT) is a measure of visuospatial scanning, attention, sequencing, and speed and executive function. Patients must "connect the dots" either in a numbered sequence or alternating letters and numbers. The TMT has two parts that are referred to as the Trail Making Test Part A and the Trail Making Test Part B. In Part A, the circles are numbered 1 - 25, and the patient should draw lines to connect the numbers in ascending order. Possible score ranges from 0-3 minutes with higher score (more seconds/minutes) indicating significant cognitive impairment. Mean change was calculated by the following formula: 100*(3 month - baseline) / baseline |
Baseline, at 3 months
|
|
Mean Change in Trail Making Test (TMT- B) Score
Временное ограничение: Baseline, at 3 months
|
Trail Making Test (TMT) is a measure of visuospatial scanning, attention, sequencing, and speed and executive function. Patients must "connect the dots" either in a numbered sequence or alternating letters and numbers. The TMT has two parts that are referred to as the Trail Making Test Part A and the Trail Making Test Part B. In Part B, the circles include both numbers (1 - 13) and letters (A - L). Possible score ranges from 0-5 minutes with higher score (more seconds/minutes) indicating significant cognitive impairment. |
Baseline, at 3 months
|
|
Mean Change in Cognitive Function as Measured by Medical Outcomes Scale (MOS)
Временное ограничение: Baseline, at 3 months
|
Medical Outcomes Scale (MOS) assess cognitive function with possible score range from 0-100, with higher scores indicating better outcome. Mean change was calculated by the following formula: 100*(3 month - baseline) / baseline |
Baseline, at 3 months
|
|
Mean Change in Cognitive Function as Measured by Mini-Mental Status Examination (MMSE)
Временное ограничение: Baseline, at 3 months
|
Mini-Mental Status Examination (MMSE) is a brief, standardized tool to grade patients' global cognitive function. Possible scores range from 0-30, with lower score indicating severe cognitive impairment. Mean change was calculated by the following formula: 100*(3 month - baseline) / baseline |
Baseline, at 3 months
|
|
Mean Change in Relative Fatigue as Measured by Multidimensional Fatigue Inventory (MFI-20) Scores
Временное ограничение: Baseline, 3 months
|
The MFI-20 is a multidimensional, self-reporting instrument designed to measure fatigue.
It covers the following dimensions: general fatigue, physical fatigue, mental fatigue, reduced motivation, and reduced activity.
Possible subscore ranges from 4 to 20 is reported for each dimension, with 20 corresponding to maximal fatigue.
|
Baseline, 3 months
|
|
Cumulative Incidence of Local Failure
Временное ограничение: 1 year
|
Cumulative incidence of local failure, defined as tumor recurrence . Percent local failure at 1 year. The Cox proportional hazards regression model will be used to evaluate Cumulative incidence of local failure. This is to evaluate local control of brain metastases treated with integrated boost. |
1 year
|
|
Cumulative Incidence of Intracranial Failure
Временное ограничение: 1 year
|
Cumulative incidence of intracranial failure was estimated by the Cox proportional hazards regression model. Intracranial failure is any failure in the brain. |
1 year
|
|
Percentage of Participants With Local Failures Within the Region of Brain Within the CTV Receiving 20 Gy
Временное ограничение: 1 year
|
Percentage of participants with local failures within the region of brain within the CTV (Clinical Target Volume ) receiving 20 Gy
|
1 year
|
|
Number of Participants With Recurrence in the Hippocampus
Временное ограничение: 5 months
|
Recurrence in the hippocampus was noted after hippocampal-sparing whole brain irradiation with simultaneous integrated boost (HSIB-WBRT)
|
5 months
|
|
Median Progression Free Survival
Временное ограничение: 39 months
|
Tumor progression is measured radiographically.
The Kaplan-Meier estimator was used to determine the median time to death for this patient population.
|
39 months
|
|
Median Overall Survival.
Временное ограничение: 39 months
|
Overall survival is measured by the Kaplan-Meier estimator used to determine the median overall survival for this patient population.
|
39 months
|
|
Number of Adverse Events Grade 3 or Higher Based on CTCAE (Common Terminology Criteria for Adverse Events) Criteria.
Временное ограничение: From start of treatment up to 39 months
|
The adverse event (AE) including any adverse event would be assessed by Common Terminology Criteria for Adverse Events (CTCAE) version 4.0
|
From start of treatment up to 39 months
|
|
Health-related Quality of Life as Assessed by the Functional Assessment of Cancer Therapy With Brain Subscale (FACT-BR)
Временное ограничение: 39 months
|
Quality of life will be assessed using the Functional Assessment of Cancer Therapy with Brain Subscale (FACT-BR). The FACT-BR is a multidimensional, self-report quality of life instrument specifically designed and validated for use with brain malignancy patients. It is written at the 4th grade reading level and can be completed in 5-10 minutes with little or no assistance in patients who are not neurologically incapacitated. It measures quality of life related to symptoms or problems across 5 scales: physical well-being (7 items); social/family well-being (7 items);emotional well-being (6 items); functional well-being (7 items); and concerns relevant to patients with brain tumors (23 items). Items are rated on a 5-point scale (0-5): 0-"not at all", 1- "a little bit", 2-"somewhat", 3-"quite a bit" and 4-"very much", with HIGHER scores indicating a better quality of life. |
39 months
|
|
Health-related Quality of Life as Assessed by Euroqol EQ-5D
Временное ограничение: 39 months
|
The EQ (Euroqol)-5D (5 Dimension) health related quality of life questionnaire is a standardized instrument for use as a measure of health outcome. Applicable to a wide range of health conditions and treatments, it provides a simple descriptive profile and a single index value for health status. . The US version of the EQ-5D will be used, to enable mapping of general HR-QoL (Health-related quality of life) scores from EQ-5D scores into health state utility scores (ranging from 0 to 1) for the US population. Possible scores range from 0 to 1, with HIGHER scores indicating a better quality of life. |
39 months
|
Соавторы и исследователи
Следователи
- Главный следователь: Robert Timmerman, MD, UT Southwestern Medical Center Dallas
Даты записи исследования
Изучение основных дат
Начало исследования (Действительный)
Первичное завершение (Действительный)
Завершение исследования (Действительный)
Даты регистрации исследования
Первый отправленный
Впервые представлено, что соответствует критериям контроля качества
Первый опубликованный (Оценивать)
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
Последнее отправленное обновление, отвечающее критериям контроля качества
Последняя проверка
Дополнительная информация
Термины, связанные с этим исследованием
Дополнительные соответствующие термины MeSH
Другие идентификационные номера исследования
- STU 042011-050
Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .